chrosomal অস্বাভাবিকতা আছে যা একটি সেল ক্রোমোজোমের স্বাভাবিক সংখ্যা বেশি হয়

trisomy's Usage Examples:

Down syndrome or Down's syndrome, also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome.

A trisomy is a type of polysomy in which there are three instances of a particular chromosome, instead of the normal two.

A trisomy is a type of aneuploidy.

Edwards syndrome, also known as trisomy 18, is a genetic disorder caused by the presence of a third copy of all or part of chromosome 18.

contains a full extra copy of chromosome 13 (a disorder known as trisomy 13 or trisomy D or T13), or because each cell contains an extra partial copy of.

Trisomy 18 (Edwards syndrome) affects 1 in 6,000 births, and trisomy 13 (Patau syndrome) affects 1 in 10,000 births.

10% of infants with trisomy 18.

It is the most common trisomy leading to miscarriage.

Full trisomy 9 is a lethal chromosomal disorder caused by having three copies (trisomy) of chromosome number 9.

It can be a viable condition if trisomy affects.

Trisomy 8 causes Warkany syndrome 2, a human chromosomal disorder caused by having three copies (trisomy) of chromosome 8.

Although most forms of trisomy are due to problems in meiosis and affect all cells of the organism, some cases occur where the trisomy occurs.

has phenotypic overlap with a number of more common disorders, such as trisomy X and Down syndrome, and diagnosis is usually unclear prior to chromosomal.

Human trisomies compatible with live birth, other than Down syndrome (trisomy 21), are Edwards syndrome (trisomy 18) and Patau syndrome (trisomy 13).

condition, a syndrome occurring in patients with mosaic trisomy 13 or translocation trisomy 13.

fetuses with trisomy 13 and trisomy 18 but not with trisomy 21.

Previous studies found elevated levels of cell-free fetal DNA for trisomy 13 and 21 from.

C15 trisomy affects twice as many males as females.

It can be associated with Edwards' syndrome (trisomy 18), Patau syndrome (trisomy 13), Trisomy 9 and mutation in the gene HOXD10.

Distal trisomy 10 is a rare chromosomal disorder that causes several physical defects and intellectual disability.

Chromosome 2, trisomy 2p Chromosome 2, Trisomy 2p13 p21 Chromosome 2, trisomy 2pter p24 Chromosome 2, trisomy 2q Chromosome 2, trisomy 2q37 Chromosome.

trisomy's Meaning':

chrosomal abnormality in which there is one more than the normal number of chromosomes in a cell